Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 658195생성일: 2026년 10월 26일
Stannous Chloride → N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-amino-1-benzofuran-2-carboxamide
https://huagongshe.com/reaction/658195
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Stannous Chloride | HCID 24479 | — |
| 반응물 | N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-nitro-1-benzofuran-2-carboxamide | HCID 59341430 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-amino-1-benzofuran-2-carboxamide | HCID 59341406 | — |
반응 단계
6.0 ml (12 mmol) of a 2 M tin(II) chloride solution in DMF are added to N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-nitro-1-benzofuran-2-carboxamide (1340 mg, 4.25 mmol). The mixture is stirred overnight. The solvent is removed under reduced pressure using a rotary evaporator. The crude product is taken up in methanol and, together with acidic ion exchange resin (Dowex WX2-200), shaken for about 1 h. The loaded ion exchanger is washed with methanol, then with water, again with methanol, with DMF, again with methanol, with THF, again with methanol, with dichloromethane and finally once more with methanol. The product is eluted with methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. 1200 mg (98% of theory) of the title compound are obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08076355B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-d5c3526cdb9248478e94d79347985c09 |
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| 출처 메모 | uspto-grants-2011_12 |
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